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Journal Abstract Search

452 related items for PubMed ID: 6511919

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  • 2. Homocystinuria and megaloblastic anemia responsive to vitamin B12 therapy. An inborn error of metabolism due to a defect in cobalamin metabolism.
    Schuh S, Rosenblatt DS, Cooper BA, Schroeder ML, Bishop AJ, Seargeant LE, Haworth JC.
    N Engl J Med; 1984 Mar 15; 310(11):686-90. PubMed ID: 6700644
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  • 3. Vitamin B12 responsive homocystinuria and megaloblastic anemia: heterogeneity in methylcobalamin deficiency.
    Rosenblatt DS, Thomas IT, Watkins D, Cooper BA, Erbe RW.
    Am J Med Genet; 1987 Feb 15; 26(2):377-83. PubMed ID: 3812589
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  • 4. New disorder of vitamin B12 metabolism (cobalamin F) presenting as methylmalonic aciduria.
    Rosenblatt DS, Laframboise R, Pichette J, Langevin P, Cooper BA, Costa T.
    Pediatrics; 1986 Jul 15; 78(1):51-4. PubMed ID: 3725502
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  • 10. Vitamin B12-responsive neonatal megaloblastic anemia and homocystinuria with associated reduced methionine synthase activity.
    Hallam LJ, Sawyer M, Clark AC, Van der Weyden MB.
    Blood; 1987 Apr 15; 69(4):1128-33. PubMed ID: 3828532
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  • 11. A cobalamin metabolic defect with homocystinuria, methylmalonic aciduria and macrocytic anemia.
    Mamlok RJ, Isenberg JN, Rassin DK, Norcross K, Tallan HH.
    Neuropediatrics; 1986 May 15; 17(2):94-9. PubMed ID: 2873525
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  • 12. Cobalamin binding and cobalamin-dependent enzyme activity in normal and mutant human fibroblasts.
    Mellman I, Willard HF, Rosenberg LE.
    J Clin Invest; 1978 Nov 15; 62(5):952-60. PubMed ID: 30783
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  • 13. Perturbation of methionine metabolism in sheep with nitrous-oxide-induced inactivation of cobalamin.
    Xue GP, Snoswell AM, Runciman WB.
    Biochem Int; 1986 Jan 15; 12(1):61-9. PubMed ID: 2868723
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  • 14. Cobalamin inactivation decreases purine and methionine synthesis in cultured lymphoblasts.
    Boss GR.
    J Clin Invest; 1985 Jul 15; 76(1):213-8. PubMed ID: 2862163
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  • 15. Development and reversion of methionine dependence in a human glioma cell line: relation to homocysteine remethylation and cobalamin status.
    Fiskerstrand T, Christensen B, Tysnes OB, Ueland PM, Refsum H.
    Cancer Res; 1994 Sep 15; 54(18):4899-906. PubMed ID: 8069855
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  • 16. Methionine synthase inactivation by nitrous oxide during methionine loading of normal human fibroblasts. Homocysteine remethylation as determinant of enzyme inactivation and homocysteine export.
    Christensen B, Ueland PM.
    J Pharmacol Exp Ther; 1993 Dec 15; 267(3):1298-303. PubMed ID: 8263793
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  • 18. Cobalamin metabolism in cultured human chorionic villus cells.
    Begley JA, Colligan PD, Chu RC, Hall CA.
    J Cell Physiol; 1993 Jul 15; 156(1):43-7. PubMed ID: 8100234
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  • 19. Recognition of two intracellular cobalamin binding proteins and their identification as methylmalonyl-CoA mutase and methionine synthetase.
    Kolhouse JF, Allen RH.
    Proc Natl Acad Sci U S A; 1977 Mar 15; 74(3):921-5. PubMed ID: 15259
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  • 20. Functional methionine synthase deficiency due to cblG disorder: a report of two patients and a review.
    Harding CO, Arnold G, Barness LA, Wolff JA, Rosenblatt DS.
    Am J Med Genet; 1997 Sep 05; 71(4):384-90. PubMed ID: 9286442
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